Combination chemotherapy with bevacizumab and S-1 for elderly patients with metastatic colorectal cancer (BASIC trial)

被引:20
作者
Yoshida, M. [1 ]
Muro, K. [2 ]
Tsuji, A. [3 ]
Hamamoto, Y. [4 ]
Yoshino, T. [5 ]
Yoshida, K. [6 ]
Shirao, K. [7 ]
Miyata, Y. [8 ]
Takahari, D. [2 ]
Takahashi, T. [6 ]
Ohtsu, A. [5 ]
机构
[1] Osaka Med Coll Hosp, Canc Chemotherapy Ctr, Takatsuki, Osaka 5698686, Japan
[2] Aichi Canc Ctr Hosp, Dept Clin Oncol, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[3] Kochi Hlth Sci Hosp, Dept Med Oncol, Kochi 7818555, Japan
[4] Tochigi Canc Ctr, Dept Med Oncol, Utsunomiya, Tochigi 3200834, Japan
[5] Natl Canc Ctr Hosp East, Dept Gastrointestinal Oncol Gastroenterol, Kashiwa, Chiba 2778577, Japan
[6] Gifu Univ, Dept Surg Oncol, Grad Sch Med, Gifu, Gifu 5011194, Japan
[7] Oita Univ, Fac Med, Dept Med Oncol, Oita 8795543, Japan
[8] Saku Cent Hosp, Dept Gastroenterol, Nagano 3840393, Japan
关键词
Bevacizumab; Colorectal cancer; Elderly; S-1; RANDOMIZED CONTROLLED-TRIAL; PHASE-3; TRIAL; OPEN-LABEL; 1ST-LINE TREATMENT; PLUS BEVACIZUMAB; NON-INFERIORITY; OXALIPLATIN; CAPECITABINE; FLUOROURACIL; LEUCOVORIN;
D O I
10.1016/j.ejca.2015.03.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Chemotherapeutic regimens for elderly patients with metastatic colorectal cancer (mCRC), such as bevacizumab combined with 5-fluorouracil (5-FU) and leucovorin, often exclude oxaliplatin and irinotecan owing to the risk of toxicity. However, treatment with infusional 5-fluorouracil and leucovorin requires percutaneous port-catheter placement and other precautions, causing unnecessary stress for patients as well as healthcare workers. Methods: We conducted a phase II study to evaluate the efficacy and safety of bevacizumab plus S-1 in elderly patients with previously untreated mCRC. Bevacizumab was given intravenously every two weeks, and S-1 was administered orally on days 1-28 of a 42-day cycle. The primary end-point was progression-free survival (PFS). The secondary end-points were time to treatment failure, response rate (RR), overall survival (OS), treatment completion status and safety. Results: From October 2007 through March 2010, 56 patients were enroled. The median PFS was 9.9 months, the median OS was 25.0 months, and the RR was 57%. The main adverse events of grade 3 or higher were hypertension (11%), diarrhoea (9%) and neutropenia (7%). Conclusion: Our results suggest that combination chemotherapy with S-1 and bevacizumab can be administered safely and continuously on an outpatient basis and is therapeutically effective in elderly patients with mCRC. (C) 2015 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:935 / 941
页数:7
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